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Subjects (1-26 of 26)
Pharmaceutical Preparations -- standards.
1
2002
Authentication of Chinese medicinal materials by DNA technology
River Edge, N.J. : World Scientific, [2002]
Rating:
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Location
Call no.
Vol.
Availability
W'PONDS
615.1351 Wan/Aoc
AVAILABLE
2
2002
Authentication of Chinese medicinal materials by DNA technology
Rating:
Electronic Resources
3
2018
Bitter pills : the global war on counterfeit drugs
Zaman, Muhammad H. (Muhammad Hamid), author
New York, NY : Oxford University Press, 2018
Rating:
Electronic Resources
4
2008
Combination products : regulatory challenges and successful product developement
Gopalaswamy, Smita.
Rating:
Electronic Resources
5
2008
Combination products : regulatory challenges and successful product developement
Gopalaswamy, Smita
Rating:
Electronic Resources
6
2020
Continuous pharmaceutical processing
Rating:
Electronic Resources
7
2013
Countering the problem of falsified and substandard drugs
Institute of Medicine (U.S.). Committee on Understanding the Global Public Health Implications of Substandard, Falsified, and Counterfeit Medical Products, author.
Washington, D.C. : National Academies Press, [2013]
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Electronic Resources
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8
2019
Data integrity and compliance : a primer for medical product manufacturers
Rodríguez Pérez, José, 1961- author.
Milwaukee, Wisconsin : ASQ Quality Press, [2019]
Rating:
Electronic Resources
9
2013
Devalued and Distrusted : Can the Pharmaceutical Industry Restore Its Broken Image?
LaMattina, John L.
Rating:
Electronic Resources
10
2012
Ensuring safe foods and medical products through stronger regulatory systems abroad
Washington, D.C. : National Academies Press, [2012]
Rating:
Electronic Resources
11
2002-
European drug report
Rating:
12
1983
FDA inspection operations manual : for drugs, devices, & cosmetics
United States. Department of Health and Human Services.
Rating:
Electronic Resources
13
2013
Global approach in safety testing : ICH guidelines explained
Rating:
Electronic Resources
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14
2007
Good manufacturing practices for pharmaceuticals
6th ed
Rating:
Electronic Resources
15
2007
Guide to microbiological control in pharmaceuticals and medical devices
Denyer, S. P.
2nd ed
Rating:
Electronic Resources
16
2009
Handbook of stability testing in pharmaceutical development : regulations, methodologies, and best practices
Rating:
Electronic Resources
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17
2010
An introduction to pharmacovigilance
Waller, Patrick, 1957 January 30-
Chichester, West Sussex ; Hoboken, NJ : Wiley-Blackwell, 2010
Rating:
18
2017
An introduction to pharmacovigilance
Waller, Patrick, 1957 January 30- author.
Second edition
Chichester, West Sussex, UK ; Hoboken, NJ : John Wiley & Sons Inc., [2017]
Rating:
Electronic Resources
19
Journal of biological standardization
[London] [Academic Press]
Rating:
20
Journal of GXP compliance
Royal Palm Beach, FL : Institute of Validation Technology
Rating:
21
1977
Layout : the design of the printed page
Hurlburt, Allen, 1910-1983.
New York : Watson-Guptill Publications, 1977
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Call no.
Vol.
Availability
MELB
686.225 HUR-L
AVAILABLE
22
2011
Pharmaceutical anti-counterfeiting : combating the real danger from fake drugs
Davison, Mark, 1968 March 1-
Hoboken, N.J. : John Wiley & Sons, [2011]
Rating:
23
2008
The pharmaceutical regulatory process
Second edition
London : Informa Healthcare, 2008
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Call no.
Vol.
Availability
MELB
KN 185.8 Ber/Prp 2008
AVAILABLE
24
2008
The pharmaceutical regulatory process
2nd ed
Rating:
Electronic Resources
25
2010
Pharmaceutical stability testing to support global markets
Rating:
Electronic Resources
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26
2011
Quality control training manual : comprehensive training guide for API, finished pharmaceutical and biotechnologies laboratories
Haider, Syed Imtiaz
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